Evidence map›Paper›PMID 34344349›Full record

ArticleBMC infectious diseases2021

Interleukin 6 as a marker of severe bacterial infection in children with sickle cell disease and fever: a case-control study.

Elena María Rincón-López, María Luisa Navarro Gómez, Teresa Hernández-Sampelayo Matos, David Aguilera-Alonso, Eva Dueñas Moreno, Jesús Saavedra-Lozano, Begoña Santiago García, María Del Mar Santos Sebastián, Marina García Morín, Cristina Beléndez Bieler and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Elena María Rincón-LópezDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain. elenarinconlopez@hotmail.com.
María Luisa Navarro GómezDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
Teresa Hernández-Sampelayo MatosDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
David Aguilera-AlonsoDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
Eva Dueñas MorenoDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
Jesús Saavedra-LozanoDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
Begoña Santiago GarcíaDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
María Del Mar Santos SebastiánDepartment of Pediatrics, Pediatric Infectious Diseases Unit, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, c/O'Donnell 48-50, 28009, Madrid, Spain.
Marina García MorínDepartment of Pediatrics, Pediatric Hematology and Oncology Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Cristina Beléndez BielerDepartment of Pediatrics, Pediatric Hematology and Oncology Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Jorge Lorente RomeroDepartment of Pediatrics, Pediatric Emergency Unit, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Elena Cela de JuliánUniversidad Complutense de Madrid, Madrid, Spain.
F-DREP Study Group
Hospital General Universitario Gregorio Marañón · ESUniversidad Complutense de Madrid · ES

Funding

European Society for Paediatric Infectious Diseases ESPID Small Grant 2017
6 · The paper itself

Abstract

backgroundEtiological diagnosis of fever in children with sickle cell disease (SCD) is often challenging. The aim of this study was to analyze the pattern of inflammatory biomarkers in SCD febrile children and controls, in order to determine predictors of severe bacterial infection (SBI).

methodsA prospective, case-control study was carried out during 3 years, including patients younger than 18 years with SCD and fever (cases) and asymptomatic steady-state SCD children (controls). Clinical characteristics and laboratory parameters, including 10 serum proinflammatory cytokines (IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-17a, IFN-γ and TNF-α) and comparisons among study subgroups were analyzed.

resultsA total of 137 patients (79 cases and 58 controls) were included in the study; 78.5% males, median age 4.1 (1.7-7.5) years. Four cases were diagnosed with SBI, 41 viral infection (VI), 33 no proven infection (NPI) and 1 bacterial-viral coinfection (the latter excluded from the subanalyses). IL-6 was significantly higher in patients with SBI than in patients with VI or NPI (163 vs 0.7 vs 0.7 pg/ml, p < 0.001), and undetectable in all controls. The rest of the cytokines analyzed did not show any significant difference. The optimal cut-off value of IL-6 for the diagnosis of SBI was 125 pg/mL, with high PPV and NPV (PPV of 100% for a prevalence rate of 5, 10 and 15% and NPV of 98.7%, 97.3% and 95.8% for those prevalences rates, respectively).

conclusionWe found that IL-6 (with a cut-off value of 125 pg/ml) was an optimal marker for SBI in this cohort of febrile SCD children, with high PPV and NPV. Therefore, given its rapid elevation, IL-6 may be useful to early discriminate SCD children at risk of SBI, in order to guide their management.

Indexed as

Anemia, Sickle CellBacterial InfectionsBiomarkersCase-Control StudiesChildChild, PreschoolFemaleHumansInfantInterleukin-6MaleProspective StudiesBiomarkersIL6 protein, humanInterleukin-6CytokinesFeverInfectionInterleukin-6Sickle cell disease

Identifiers

PMID34344349
PMCPMC8329904
OpenAlexW3137949568

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.